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Picoline based-homogeneous liquid–liquid microextraction of cobalt(II) and nickel(II) at trace levels from a high volume of an aqueous sample

机译:从大体积含水样品中以痕量水平进行基于皮克林的钴(II)和镍(II)的均匀液-液微萃取

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A new homogeneous liquid–liquid microextraction method using 3-picoline has been developed for preconcentration and extraction of cobalt(II) and nickel(II) ions from a high volume of an aqueous sample. In the proposed method, 3-picoline is simultaneously used as a complexing agent and an extraction solvent. Initially to 25 mL of the aqueous sample containing the analytes, 3-picoline is added to complex the studied cations. Then sodium chloride is added to this homogeneous solution. After manual shaking, the tube is placed in a water bath. Due to the decrease of 3-picoline solubility in water at high temperatures, a cloudy solution is formed. The fine droplets of 3-picoline containing cation–picoline complexes are collected on the top of the aqueous phase by centrifuging. The enriched analytes in the upper phase are determined by graphite furnace atomic absorption spectrometry. Several variables possibly affecting the extraction efficiency were investigated and optimized. Under the optimum conditions the calibration curves were linear in the ranges of 10–150 and 5–125 ng L?1 for cobalt(II) and nickel(II), respectively. The detection limits were obtained to be 3.8 and 2.2 ng L?1 for cobalt(II) and nickel(II), respectively. Finally, the proposed method has been successfully applied for simultaneous analysis of the analytes in different environmental aqueous samples.
机译:已开发出一种新的使用3-甲基吡啶的均相液-液微萃取方法,用于从大量含水样品中预富集和萃取钴(II)和镍(II)离子。在所提出的方法中,将3-甲基吡啶同时用作络合剂和萃取溶剂。最初,在25 mL含有分析物的水性样品中,添加3-picoline以络合研究的阳离子。然后将氯化钠加入该均匀溶液中。手动摇动后,将试管置于水浴中。由于高温下3-甲基吡啶在水中的溶解度降低,形成浑浊的溶液。含有3-picoline的阳离子-picoline复合物的细小液滴通过离心收集在水相的顶部。上层相中富集的分析物通过石墨炉原子吸收光谱法测定。研究和优化了可能影响提取效率的几个变量。在最佳条件下,钴(II)和镍(II)的校准曲线在10–150 ng L?1和5–125 ng L?1范围内呈线性关系。钴(II)和镍(II)的检出限分别为3.8和2.2 ng L?1。最后,所提出的方法已成功地用于同时分析不同环境水样中的分析物。

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